BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

135 related articles for article (PubMed ID: 9450893)

  • 1. Reply to "lymphoproliferative disorders in Sotos syndrome: observation in two cases".
    Cole T; Allanson J
    Am J Med Genet; 1998 Jan; 75(2):226-7. PubMed ID: 9450893
    [No Abstract]   [Full Text] [Related]  

  • 2. Lymphoproliferative disorders in Sotos syndrome: observation of two cases.
    Corsello G; Giuffrè M; Carcione A; Cuzto ML; Piccione M; Ziino O
    Am J Med Genet; 1996 Sep; 64(4):588-93. PubMed ID: 8870927
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The MIller-Dieker syndrome.
    Jones KL; Gilbert EF; Kaveggia EG; Opitz JM
    Pediatrics; 1980 Aug; 66(2):277-81. PubMed ID: 7402813
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Simpson-Golabi-Behmel syndrome. A new overgrowth syndrome with increased risk of tumor development].
    Weidle B; Orstavik KH
    Tidsskr Nor Laegeforen; 1998 Apr; 118(10):1556-8. PubMed ID: 9615582
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The Weaver syndrome: a rare type of primordial overgrowth.
    Majewski F; Ranke M; Kemperdick H; Schmidt E
    Eur J Pediatr; 1981 Nov; 137(3):277-82. PubMed ID: 7318839
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [The lesions associated with leprechaunism (author's transl)].
    Lebreuil G; Pizzi M; Sebaoun M; Oddou JH
    Arch Anat Cytol Pathol; 1980; 28(5):310-6. PubMed ID: 7447519
    [No Abstract]   [Full Text] [Related]  

  • 7. Juvenile hyaline fibromatosis with skull-encephalic anomalies: a case report and review of the literature.
    Gilaberte Y; González-Mediero I; López Barrantes V; Zambrano A
    Dermatology; 1993; 187(2):144-8. PubMed ID: 8358106
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Russell-Silver syndrome].
    Kosaki K; Izumi K; Hasegawa T
    Nihon Rinsho; 2006 Sep; Suppl 3():436-9. PubMed ID: 17022582
    [No Abstract]   [Full Text] [Related]  

  • 9. Costello syndrome: an overview.
    Hennekam RC
    Am J Med Genet C Semin Med Genet; 2003 Feb; 117C(1):42-8. PubMed ID: 12561057
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Aarskog syndrome: significance for the surgeon.
    Andrassy RJ; Murthy S; Woolley MM
    J Pediatr Surg; 1979 Aug; 14(4):462-4. PubMed ID: 39985
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The Coffin-Lowry syndrome.
    Young ID
    J Med Genet; 1988 May; 25(5):344-8. PubMed ID: 3290491
    [No Abstract]   [Full Text] [Related]  

  • 12. Ring chromosome 15 syndrome.
    Fryns JP; Timmermans J; Hondt FD; François B; Emmery L; van den Berghe H
    Hum Genet; 1979 Sep; 51(1):43-8. PubMed ID: 500090
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Risk of malignancy in Sotos syndrome.
    Hersh JH; Cole TR; Bloom AS; Bertolone SJ; Hughes HE
    J Pediatr; 1992 Apr; 120(4 Pt 1):572-4. PubMed ID: 1552397
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Two male sibs with a previously unrecognized syndrome: facial dysmorphia, hyperextensibility of joints, clinodactyly, growth retardation and mental retardation.
    Morillo-Cucci G; Passarge E; Simpson JL; Chaganti RS; German J
    Birth Defects Orig Artic Ser; 1975; 11(2):380-3. PubMed ID: 1227554
    [No Abstract]   [Full Text] [Related]  

  • 15. Sotos syndrome.
    Cole TR; Hughes HE
    J Med Genet; 1990 Sep; 27(9):571-6. PubMed ID: 2231650
    [No Abstract]   [Full Text] [Related]  

  • 16. Spectrum of NSD1 gene mutations in southern Chinese patients with Sotos syndrome.
    Tong TM; Hau EW; Lo IF; Chan DH; Lam ST
    Chin Med J (Engl); 2005 Sep; 118(18):1499-506. PubMed ID: 16232326
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cohen syndrome is neither uncommon nor new.
    Norio R
    Am J Med Genet; 1994 Nov; 53(2):202-3. PubMed ID: 7856650
    [No Abstract]   [Full Text] [Related]  

  • 18. Report of another family with Simpson-Golabi-Behmel syndrome and a review of the literature.
    Garganta CL; Bodurtha JN
    Am J Med Genet; 1992 Sep; 44(2):129-35. PubMed ID: 1456279
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Familial white matter hypoplasia, agenesis of the corpus callosum, mental retardation and growth deficiency: a new distinctive syndrome.
    Curatolo P; Cilio MR; Del Giudice E; Romano A; Gaggero R; Pessagno A
    Neuropediatrics; 1993 Apr; 24(2):77-82. PubMed ID: 8327066
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Multiple pterygium syndrome in children. 7 cases].
    Fenoll B; Rigault P; Maroteaux P; Padovani JP; Guyonvarch G; Durand Y
    Rev Chir Orthop Reparatrice Appar Mot; 1990; 76(2):102-11. PubMed ID: 2142314
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.